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Two measures of systemic inflammation are positively associated with haemoglobin levels in adolescent girls living in rural India: a cross‐sectional study

Tropical medicine & international health, 2021-03, Vol.26 (3), p.327-334

2021

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Sulphasalazine in the treatment of rheumatoid arthritis in India

Journal of the Association of Physicians of India, 1988-05, Vol.36 (5), p.350

1988

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Co-infections with chikungunya virus and dengue virus in Delhi, India

Emerging infectious diseases, 2009-07, Vol.15 (7), p.1077-1080

2009

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CSI clinical practice guidelines for dyslipidemia management: Executive summary

Indian heart journal, 2024-03, Vol.76 (Suppl 1), p.S6-S19

2024

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Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohort

Clinical genetics, 2015-02, Vol.87 (2), p.161-166

2015

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Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation

The Cleft palate-craniofacial journal, 2022-11, Vol.59 (11), p.1329-1339

2022

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Analysis of dengue specific memory B cells, neutralizing antibodies and binding antibodies in healthy adults from India

International journal of infectious diseases, 2019-07, Vol.84, p.S57-S63

2019

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Reduced Susceptibility to Ciprofloxacin and gyrA Gene Mutation in North Indian Strains of Salmonella enterica Serotype Typhi and Serotype Paratyphi A

Microbial drug resistance (Larchmont, N.Y.), 2004-06, Vol.10 (2), p.146-153

2004

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Groundwater Law and Management in India: From an Elitist to an Egalitarian Paradigm

1st Edition 2021, 2021

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Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness

American journal of human genetics, 2006-01, Vol.78 (1), p.137-143

2006

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Surveillance of transmitted HIV type 1 drug resistance among HIV type 1-positive women attending an antenatal clinic in Kakinada, India

AIDS research and human retroviruses, 2011-12, Vol.27 (12), p.1291-1297

2011

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Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study

Journal of Translational Genetics and Genomics, 2020

2020

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An Optimal Capillary Screen Cut-off of Thyroid Stimulating Hormone for Diagnosing Congenital Hypothyroidism: Data from a Pilot Newborn Screening Program in Delhi

Indian pediatrics, 2019-04, Vol.56 (4), p.281-286

2019

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Concerns on the dosing of antitubercular drugs for children in RNTCP

Indian pediatrics, 2008-10, Vol.45 (10), p.852-854

2008

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Montelukast vs. Inhaled Low-Dose Budesonide as Monotherapy in the Treatment of Mild Persistent Asthma: A Randomized Double Blind Controlled Trial

Journal of tropical pediatrics (1980), 2007-10, Vol.53 (5), p.325-330

2007

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Nested PCR Assay for Eight Pathogens: A Rapid Tool for Diagnosis of Bacterial Meningitis

Molecular diagnosis & therapy, 2016-02, Vol.20 (1), p.45-54

2016

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Gene symbol: ATP7B

Human genetics, 2007-02, Vol.120 (6), p.908-908

2007

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Superior Mediastinal Syndrome Due to Intrathoracic Tuberculosis

Indian journal of pediatrics, 2010-09, Vol.77 (9), p.1021-1023

2010

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Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism: Indian experience

Annals of hematology, 2003-07, Vol.82 (7), p.427-430

2003

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Factor VIII gene polymorphisms in the Asian Indian population

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-11, Vol.6 (6), p.625-630

2000

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Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Journal of Pediatric Endocrinology and Metabolism, 2001-01, Vol.14 (1), p.27

2001

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What is happening to caesarean section rates?

The Lancet (British edition), 1994-01, Vol.343 (8890), p.179-180

1994

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Juvenile dermatomyositis

Indian journal of pediatrics, 1996-05, Vol.63 (3), p.375-379

1996

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Prenatal diagnosis of haemoglobinopathies

The National medical journal of India, 2001-11, Vol.14 (6), p.340-342

2001

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Governance reform for vision India

Indian journal of public administration, 2006, Vol.LII (2), p.289-291

2006

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Two measures of systemic inflammation are positively associated with haemoglobin levels in adolescent girls living in rural India: a cross‐sectional study

Sulphasalazine in the treatment of rheumatoid arthritis in India

Co-infections with chikungunya virus and dengue virus in Delhi, India

CSI clinical practice guidelines for dyslipidemia management: Executive summary

Mutation spectrum in BBS genes guided by homozygosity mapping in an Indian cohort

Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation

Analysis of dengue specific memory B cells, neutralizing antibodies and binding antibodies in healthy adults from India

Reduced Susceptibility to Ciprofloxacin and gyrA Gene Mutation in North Indian Strains of Salmonella enterica Serotype Typhi and Serotype Paratyphi A

Groundwater Law and Management in India: From an Elitist to an Egalitarian Paradigm

Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness

Surveillance of transmitted HIV type 1 drug resistance among HIV type 1-positive women attending an antenatal clinic in Kakinada, India

Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study

An Optimal Capillary Screen Cut-off of Thyroid Stimulating Hormone for Diagnosing Congenital Hypothyroidism: Data from a Pilot Newborn Screening Program in Delhi

Concerns on the dosing of antitubercular drugs for children in RNTCP

Montelukast vs. Inhaled Low-Dose Budesonide as Monotherapy in the Treatment of Mild Persistent Asthma: A Randomized Double Blind Controlled Trial

Nested PCR Assay for Eight Pathogens: A Rapid Tool for Diagnosis of Bacterial Meningitis

Gene symbol: ATP7B

Superior Mediastinal Syndrome Due to Intrathoracic Tuberculosis

Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism: Indian experience

Factor VIII gene polymorphisms in the Asian Indian population

Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

What is happening to caesarean section rates?

Juvenile dermatomyositis

Prenatal diagnosis of haemoglobinopathies

Governance reform for vision India

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